(S)-[1-benzyl-2-(2-bromobenzyloxy)-ethyl]-(2-bromo-4,5-dimethoxy-benzyl)-methyl-amine | 286687-94-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (S)-[1-benzyl-2-(2-bromobenzyloxy)-ethyl]-(2-bromo-4,5-dimethoxy-benzyl)-methyl-amine
• 英文别名: (2S)-N-[(2-bromo-4,5-dimethoxyphenyl)methyl]-1-[(2-bromophenyl)methoxy]-N-methyl-3-phenylpropan-2-amine
• CAS: 286687-94-3
• 化学式: C₂₆H₂₉Br₂NO₃
• 分子量: 563.329
• InChiKey: ZYKRCXINNUEWOU-QFIPXVFZSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.5
• 重原子数：
  32
• 可旋转键数：
  11
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  30.9
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (S)-[1-benzyl-2-(2-bromobenzyloxy)-ethyl]-(2-bromo-4,5-dimethoxy-benzyl)-methyl-amine 在 叔丁基锂 、 1,3-二硝基苯 作用下， 以 various solvent(s) 为溶剂， 以92%的产率得到(S)-8-Benzyl-12,13-dimethoxy-9-methyl-7,8,9,10-tetrahydro-5H-6-oxa-9-aza-dibenzo[a,c]cyclodecene
  参考文献：
  名称：

  面向多样性、立体选择性合成含双芳基或双（芳基）金属的中环

  摘要：

  实验技术和装置除非另有说明，反应在氩气下用干燥的、新鲜蒸馏的溶剂进行。从钠/二苯甲酮羰基中蒸馏出四氢呋喃。无水 2-甲基四氢呋喃（Aldrich，外消旋）储存在活化的分子筛上。从氢化钙中蒸馏出二氯甲烷。正丁基锂的己烷溶液 (Aldrich) 和叔丁基锂的戊烷溶液 (Aldrich) 在使用前用 1,10 菲咯啉和无水 2-丁醇滴定。所有其他试剂均按照“实验室化学品的纯化”中的说明进行纯化或使用从商业来源获得的。产率是指色谱和光谱纯的化合物。所有反应均通过薄层色谱法 (TLC) 使用预涂有大肠杆菌的玻璃板进行监测。默克硅胶 60 F254 或氧化铝 60 F254。通过紫外荧光猝灭（λmax = 254nm）或用钼酸铈铵或 Dragendorff's 试剂（0.08% w/v 次硝酸铋和 2% w/v KI 的 3M aq. AcOH）染色进行可视化。保留因子 (Rf) 引用为 0.01。熔点是使用

  DOI：

  10.1021/ja0010507
• 作为产物：
  描述：

  6-溴藜芦醛 在 甲酸 、 sodium hydride 作用下， 以 四氢呋喃 、 甲醇 、 氯仿 、 水 为溶剂， 反应 5.5h， 生成 (S)-[1-benzyl-2-(2-bromobenzyloxy)-ethyl]-(2-bromo-4,5-dimethoxy-benzyl)-methyl-amine
  参考文献：
  名称：

  Diversity-Oriented Synthesis of Biaryl-Containing Medium Rings Using a One Bead/One Stock Solution Platform

  摘要：

  Diversity-oriented synthesis of structurally complex and diverse small molecules can be used as the first step in a process to explore cellular and organismal pathways. The success of this process is likely going to be dependent on advances in the synthesis of small molecules having natural product-like structures in an efficient and stereoselective manner. The development, scope, and mechanism of the oxidation of organocuprates was investigated and exploited in the atropdiastereoselective synthesis of biaryl-containing medium rings (9-, 10-, and 11-membered rings). The methodology was performed on high-capacity, large polystyrene beads by metalating aryl bromides with i-PrBu2MgLi, followed by transmetalating with CuCN.2LiBr and then oxidizing with 1,3-dinitrobenzene, and was used in a diversity-oriented synthesis of biaryl-containing medium rings (library total theoretical maximum 1412 members). The high capacity beads were arrayed into 384-well plates and, using a process optimized during the development of a one bead/one stock solution technology platform, converted into arrays of stock solutions, with each stock solution containing largely one compound. These stock solutions were used in numerous phenotypic and protein-binding assays. The process described outlines a pathway that we feel will contribute to a comprehensive and systematic chemical approach to exploring biology (chemical genetics).

  DOI：

  10.1021/ja017248o